Skip to main content Accessibility help
×
Hostname: page-component-77c89778f8-swr86 Total loading time: 0 Render date: 2024-07-16T12:06:11.233Z Has data issue: false hasContentIssue false

20 - Acute lymphoblastic leukemia in the elderly patient: diagnosis and therapy

from Part IV - Hematologic malignancies and aging

Published online by Cambridge University Press:  21 October 2009

Lodovico Balducci
Affiliation:
H. Lee Moffitt Cancer Center & Research Institute, Florida
William Ershler
Affiliation:
Institute for Advanced Studies in Aging and Geriatric Medicine, Washington DC
Giovanni de Gaetano
Affiliation:
Catholic University, Campobasso
Get access

Summary

Epidemiology

In adults, acute lymphoblastic leukemia (ALL) is a rare disease with a poor prognosis. An estimated 3970 new cases of ALL (all ages) were diagnosed in the USA during 2005. The incidence of the disease peaks in the age group 1 to 4 years, with 7.2 cases per 100 000. From ages 20 to 60 years the incidence decreases to less than 1 per 100 000. A secondary increase is noted after age 60, peaking at age 85+ with 1.6 cases expected per 100 000. Among adults, approximately 30% of ALL cases arise in patients aged 60 years or older.

Similar findings have been reported from other countries, such as the population-based study by Taylor and coworkers from the Northern Health Region of England (approximately 3 million people). Over the 8.5-year study period, 157 cases of ALL in adults (age >15) were identified. Of these cases, 31% were individuals aged over 60 (annual incidence 0.9 per 100 000). In the Western Swedish Health Care Region, the incidence of ALL was 0.72 per 100 000 in patients over the age of 65 (1982–96). In this study, the three-year overall survival (OS) rate for elderly ALL patients was 14.2%. These data are similar to those reported by SEER in the USA: a five-year OS rate of 7.9% for individuals age 65 or older.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×